Angela Matchan
Overview
Explore the profile of Angela Matchan including associated specialties, affiliations and a list of published articles.
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17
Citations
1188
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Recent Articles
1.
Smedley D, Smith K, Martin A, Thomas E, McDonagh E, Cipriani V, et al.
N Engl J Med
. 2021 Nov;
385(20):1868-1880.
PMID: 34758253
Background: The U.K. 100,000 Genomes Project is in the process of investigating the role of genome sequencing in patients with undiagnosed rare diseases after usual care and the alignment of...
2.
Farmaki A, Rayner N, Kafyra M, Matchan A, Ntaoutidou K, Feritoglou P, et al.
Nutrients
. 2019 Dec;
11(12).
PMID: 31847144
The present study describes the geographically isolated Pomak population and its particular dietary patterns in relationship to cardiovascular risk factors. We collected a population-based cohort in a cross-sectional study, with...
3.
Picco G, Chen E, Alonso L, Behan F, Goncalves E, Bignell G, et al.
Nat Commun
. 2019 May;
10(1):2198.
PMID: 31097696
Many gene fusions are reported in tumours and for most their role remains unknown. As fusions are used for diagnostic and prognostic purposes, and are targets for treatment, it is...
4.
Iotchkova V, Huang J, Morris J, Jain D, Barbieri C, Walter K, et al.
Nat Genet
. 2018 Nov;
50(12):1752.
PMID: 30390057
In the version of the article published, the surname of author Aaron Isaacs is misspelled as Issacs.
5.
Garcia-Alonso L, Iorio F, Matchan A, Fonseca N, Jaaks P, Peat G, et al.
Cancer Res
. 2017 Dec;
78(3):769-780.
PMID: 29229604
Transcriptional dysregulation induced by aberrant transcription factors (TF) is a key feature of cancer, but its global influence on drug sensitivity has not been examined. Here, we infer the transcriptional...
6.
Tachmazidou I, Suveges D, Min J, Ritchie G, Steinberg J, Walter K, et al.
Am J Hum Genet
. 2017 May;
100(6):865-884.
PMID: 28552196
Deep sequence-based imputation can enhance the discovery power of genome-wide association studies by assessing previously unexplored variation across the common- and low-frequency spectra. We applied a hybrid whole-genome sequencing (WGS)...
7.
Southam L, Gilly A, Suveges D, Farmaki A, Schwartzentruber J, Tachmazidou I, et al.
Nat Commun
. 2017 May;
8:15606.
PMID: 28548082
Next-generation association studies can be empowered by sequence-based imputation and by studying founder populations. Here we report ∼9.5 million variants from whole-genome sequencing (WGS) of a Cretan-isolated population, and show...
8.
Farmaki A, Rayner N, Matchan A, Spiliopoulou P, Gilly A, Kariakli V, et al.
Public Health Nutr
. 2016 Dec;
20(6):1063-1074.
PMID: 27989266
Objective: We carried out de novo recruitment of a population-based cohort (MANOLIS study) and describe the specific population, which displays interesting characteristics in terms of diet and health in old...
9.
Iotchkova V, Huang J, Morris J, Jain D, Barbieri C, Walter K, et al.
Nat Genet
. 2016 Sep;
48(11):1303-1312.
PMID: 27668658
Large-scale whole-genome sequence data sets offer novel opportunities to identify genetic variation underlying human traits. Here we apply genotype imputation based on whole-genome sequence data from the UK10K and 1000...
10.
Surendran P, Drenos F, Young R, Warren H, Cook J, Manning A, et al.
Nat Genet
. 2016 Sep;
48(10):1151-1161.
PMID: 27618447
High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics...